Hypertrichosis
Symptom Information:
Symptom ID: | HPO:0000998 | |||||||||||||||||||
Synonyms: |
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Cross references: |
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Is a (Direct Parents): |
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Is a (Whole tree): |
HPO:
All(HPO:0000001) Phenotypic abnormality(HPO:0000118) Abnormality of the integument(HPO:0001574) Abnormality of skin adnexa(HPO:0011138) Abnormality of the hair(HPO:0001595) Abnormal hair quantity(HPO:0011362) Hypertrichosis(HPO:0000998) MedDRA: Skin and subcutaneous tissue disorders(MedDRA:10040785) Skin appendage conditions(MedDRA:10040798) Hypertrichoses(MedDRA:10020863) Hypertrichosis(HPO:0000998) |
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Database Frequency: | 52 / 7739 | |||||||||||||||||||
Resource: |
All diseases associated with this symptom:
17q12 microdeletion syndrome | (Orphanet:261265) |
Adducted thumbs - arthrogryposis, Christian type | (Orphanet:2952) |
Alpha-mannosidosis | (Orphanet:61) |
Alström syndrome | (Orphanet:64) |
Autosomal recessive spastic paraplegia type 53 | (Orphanet:319199) |
Barber-Say syndrome | (Orphanet:1231) |
Bardet-Biedl syndrome | (Orphanet:110) |
Berardinelli-Seip congenital lipodystrophy | (Orphanet:528) |
Bloom syndrome | (Orphanet:125) |
Carney complex | (Orphanet:1359) |
Congenital erythropoietic porphyria | (Orphanet:79277) |
Congenital lactic acidosis, Saguenay-Lac-St. Jean type | (Orphanet:70472) |
Congenital reticular ichthyosiform erythroderma | (Orphanet:281190) |
Cushing disease | (Orphanet:96253) |
Cushing syndrome | (Orphanet:553) |
Dahlberg-Borer-Newcomer syndrome | (Orphanet:1563) |
Familial partial lipodystrophy associated with PPARG mutations | (Orphanet:79083) |
Familial partial lipodystrophy, Dunnigan type | (Orphanet:2348) |
Filippi syndrome | (Orphanet:3255) |
GM1 gangliosidosis | (Orphanet:354) |
GM1 gangliosidosis type 1 | (Orphanet:79255) |
Gingival fibromatosis-hypertrichosis syndrome | (Orphanet:2026) |
Gorlin-Chaudhry-Moss syndrome | (Orphanet:2095) |
HYPERTRICHOSIS, HYPERKERATOSIS, MENTAL RETARDATION, AND DISTINCTIVEFACIAL FEATURES | (OMIM:609943) |
Hurler syndrome | (Orphanet:93473) |
Insulin-resistance syndrome type A | (Orphanet:2297) |
LIPODYSTROPHY, CONGENITAL GENERALIZED, TYPE 1 | (OMIM:608594) |
LIPODYSTROPHY, CONGENITAL GENERALIZED, TYPE 2 | (OMIM:269700) |
LIPODYSTROPHY, CONGENITAL GENERALIZED, TYPE 3 | (OMIM:612526) |
Leigh syndrome | (Orphanet:506) |
Leprechaunism | (Orphanet:508) |
MELAS | (Orphanet:550) |
MENTAL RETARDATION, AUTOSOMAL DOMINANT 27 | (OMIM:615866) |
Marshall-Smith syndrome | (Orphanet:561) |
Morgagni-Stewart-Morel syndrome | (Orphanet:77296) |
Mucopolysaccharidosis type 2 | (Orphanet:580) |
Mullerian derivatives - lymphangiectasia - polydactyly | (Orphanet:1655) |
PORPHYRIA CUTANEA TARDA, TYPE I | (OMIM:176090) |
Partial acquired lipodystrophy | (Orphanet:79087) |
Polycystic ovaries - urethral sphincter dysfunction | (Orphanet:2795) |
Pontocerebellar hypoplasia type 8 | (Orphanet:324569) |
Porphyria cutanea tarda | (Orphanet:101330) |
Rabson-Mendenhall syndrome | (Orphanet:769) |
Ramon syndrome | (Orphanet:3019) |
SRD5A3-CDG | (Orphanet:324737) |
Schinzel-Giedion syndrome | (Orphanet:798) |
Sporadic Leigh syndrome | (Orphanet:255199) |
TENORIO SYNDROME | (OMIM:616260) |
TMCO1 defect syndrome | (Orphanet:228407) |
Transaldolase deficiency | (Orphanet:101028) |
Wilson-Turner syndrome | (Orphanet:3459) |
Zimmermann-Laband syndrome | (Orphanet:3473) |